Canonical Allele Identifier: CA2612834585

Gene: NELL1

Linked Data

• gnomAD v4: 11-20783839-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783842_20783843del , CM000673.2:g.20783842_20783843del	GRCh38
NC_000011.9:g.20805388_20805389del , CM000673.1:g.20805388_20805389del	GRCh37
NC_000011.8:g.20761964_20761965del	NCBI36
NG_047064.1:g.119292_119293del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.335+12_335+13del MANE Select	ENSP00000349654.5:n.335+12_335+13del
ENST00000298925.9:c.419+12_419+13del	ENSP00000298925.5:n.419+12_419+13del
ENST00000325319.9:c.335+12_335+13del	ENSP00000317837.5:n.335+12_335+13del
ENST00000357134.9:c.335+12_335+13del	ENSP00000349654.5:n.335+12_335+13del
ENST00000524738.1:n.162+12_162+13del
ENST00000527873.5:n.356+12_356+13del
ENST00000528046.5:n.518+12_518+13del
ENST00000529595.1:n.223+12_223+13del
ENST00000532434.5:c.335+12_335+13del	ENSP00000437170.1:n.335+12_335+13del
ENST00000619031.4:c.-378+12_-378+13del	ENSP00000479479.1:n.-378+12_-378+13del
NM_001288713.1:c.419+12_419+13del	NP_001275642.1:n.419+12_419+13del
NM_001288714.1:c.335+12_335+13del	NP_001275643.1:n.335+12_335+13del
NM_006157.4:c.335+12_335+13del	NP_006148.2:n.335+12_335+13del
NM_201551.2:c.335+12_335+13del	NP_963845.1:n.335+12_335+13del
NM_006157.5:c.335+12_335+13del MANE Select	NP_006148.2:n.335+12_335+13del